Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 4:6303606 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM982042

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

4:g.6303606G>T
ENST00000507765.1:n.2269G>T
ENST00000503569.1:c.2084G>T
ENSP00000423337.1:p.Gly695Val
ENST00000226760.1:c.2084G>T
ENSP00000226760.1:p.Gly695Val

Variation displays